Methods and compositions related to mutant kunitz domain i of tfpi-2

ABSTRACT

Disclosed are methods and compositions relating to plasmin inhibition.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH

This invention was made with government support under NIH Grants HL-70369, HL 64119, and HL-36365. Therefore, the United States Government may have certain rights in this invention.

STATEMENT REGARDING SEQUENCE LISTING

The Sequence Listing associated with this application is provided in text format in lieu of a paper copy, and is hereby incorporated by reference into the specification. The name of the text file containing the Sequence Listing is 720156_(—)401D1_SEQUENCE_LISTING.txt. The text file is 3.9 KB, was created on Feb. 4, 2015, and is being submitted electronically via EFS-Web.

BACKGROUND OF THE INVENTION

The agent mainly responsible for fibrinolysis is plasmin, the activated form of plasminogen. Many substances can activate plasminogen, including activated Hageman factor, streptokinase, urokinase (uPA), tissue-type plasminogen activator (tPA), and plasma kallikrein (pKA). pKA is both an activator of the zymogen form of urokinase and a direct plasminogen activator.

Plasmin is undetectable in normal circulating blood, but plasminogen, the zymogen, is present at about 3 μM. An additional, unmeasured amount of plasminogen is bound to fibrin and other components of the extracellular matrix and cell surfaces. Normal blood contains the physiological inhibitor of plasmin, α2-plasmin inhibitor (α2-PI), at about 2 μM. Plasmin and α2-PI form a 1:1 complex. Matrix or cell bound-plasmin is relatively inaccessible to inhibition by α2-PI. Thus, activation of plasmin can exceed the neutralizing capacity of α2-PI causing a profibrinolytic state.

Plasmin, once formed, degrades fibrin clots, sometimes prematurely; digests fibrinogen (the building material of clots) impairing hemostasis by causing formation of friable, easily lysed clots from the degradation products, and inhibition of platelet adhesion/aggregation by the fibrinogen degradation products; interacts directly with platelets to cleave glycoproteins Ib and IIb/IIIa preventing adhesion to injured endothelium in areas of high shear blood flow and impairing the aggregation response needed for platelet plug formation (ADEL86); proteolytically inactivates enzymes in the extrinsic coagulation pathway further promoting a prolytic state.

Inappropriate fibrinolysis and fibrinogenolysis leading to excessive bleeding is a frequent complication of surgical procedures that require extracorporeal circulation, such as cardiopulmonary bypass, and is also encountered in thrombolytic therapy and organ transplantation, particularly liver. Other clinical conditions characterized by high incidence of bleeding diathesis include liver cirrhosis, amyloidosis, acute promyelocytic leukemia, and solid tumors. Restoration of hemostasis requires infusion of plasma and/or plasma products, which risks immunological reaction and exposure to pathogens, e.g. hepatitis virus and HIV.

Very high blood loss can resist resolution even with massive infusion. When judged life-threatening, the hemorrhage is treated with antifibrinolytics such as ε-amino caproic acid (See HOOV93) (EACA), tranexamic acid, or aprotinin (NEUH89). Aprotinin is also known as Trasylol® and as Bovine Pancreatic Trypsin Inhibitor (BPTI). Hereinafter, aprotinin will be referred to as “BPTI.” EACA and tranexamic acid only prevent plasmin from binding fibrin by binding the kringles, thus leaving plasmin as a free protease in plasma. BPTI is a direct inhibitor of plasmin and is the most effective of these agents. Due to the potential for thrombotic complications, renal toxicity and, in the case of BPTI, immunogenicity, these agents are used with caution and usually reserved as a “last resort” (PUTT89). All three of the antifibrinolytic agents lack target specificity and affinity and interact with tissues and organs through uncharacterized metabolic pathways. The large doses required due to low affinity, side effects due to lack of specificity and potential for immune reaction and organ/tissue toxicity augment against use of these antifibrinolytics prophylactically to prevent bleeding or as a routine postoperative therapy to avoid or reduce transfusion therapy. Thus, there is a need for a safe antifibrinolytic.

Excessive bleeding can result from deficient coagulation activity, elevated fibrinolytic activity, or a combination of the two conditions. In most bleeding diatheses one must control the activity of plasmin. The clinically beneficial effect of bovine pancreatic trypsin inhibitor (BPTI) in reducing blood loss is thought to result from its inhibition of plasmin (Kd approximately 0.3 nM) or of plasma kallikrein (Kd approximately 100 nM) or both enzymes.

Interestingly, BPTI-induced hypersensitivity reaction occurs in about 1.2 to 2.7 percent of patients reexposed to aprotinin (30). Of these reactions 50 percent are life threatening with 9 percent fatality rate (30). Thus, a human molecule that is selectively modified to make it more potent is highly desirable. Such molecule is also expected to be less immunogenic. Side effects and toxicity issues for the use of BPTI have recently been outlined (Manago et al., N Engl J Med 2006; 354:353-65). Textilinin has also been compared with aprotinin, however, textilinin is a snake protein and therefore has immunogenecity issues associated with it. (Pathophysiol Haemost Thromb. 2005; 34 (4-5): 188-93 and U.S. Pat. No. 7,070,969).

What is needed in the art is a plasmin inhibitor that is as potent (or more potent) than BPTI, but that is almost identical to a human protein domain, thereby offering similar therapeutic potential but posing less potential for antigenicity.

SUMMARY OF THE INVENTION

In accordance with the purpose(s) of this invention, as embodied and broadly described herein, this invention, in one aspect, relates to a polypeptide comprising SEQ ID NO:1 with one or more mutations. For example, provided herein is SEQ ID NO:1 with one or more of the following substitutions: leucine is changed to arginine or lysine at position 17 (BPTI numbering); tyrosine is changed to glutamic acid at position 46; tyrosine is changed to threonine at position 11; aspartic acid is changed to tyrosine or glutamic acid at position 10; alanine is changed to methionine at position 16; alanine is changed to glycine at position 16; alanine is changed to serine at position 16.

Also disclosed herein are the polypeptides that inhibit plasmin. Also disclosed herein are polypeptides that inhibit plasmin and have reduced anticoagulation activity compared to the wild type Kunitz domain of TFPI-2. Also disclosed herein are polypeptides that are specific as antifibrinolytic agents.

Also disclosed are compositions comprising the polypeptides discussed herein.

Also disclosed are nucleic acids encoding the polypeptides disclosed herein.

Also disclosed are methods of inhibiting at least one activity of plasmin comprising contacting plasmin with an effective amount of a polypeptide disclosed herein.

Also disclosed is a method of treating a subject in need of inhibition of a plasmin activity, comprising administering to the subject an effective amount of a polypeptide disclosed herein. Examples of diseases, disorders, and treatments relating to the need of inhibition of plasmin include, but are not limited to, tumorogenesis, angiogenesis, bone remodeling, surgery, hemophilia, orthopedic surgery, coronary artery bypass grafting (CABG), and systemic inflammatory response syndrome (SIRS).

Also disclosed is a method of treating rheumatoid arthritis in a subject in need thereof, comprising administering to the subject an effective amount of a polypeptide disclosed herein.

Also disclosed is a method of identifying a plasmin inhibitor comprising: modeling a crystal structure of plamsin with a variant of KD1; determining interaction between the plasmin and the variant of KD1; based on results of the interaction, determining if the variant of KD1 is a plasmin inhibitor.

Also disclosed is a method of inhibiting plasmin in a subject in need thereof comprising administering to the subject an effective amount of the nucleic acid disclosed herein.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments of the invention and together with the description, serve to explain the principles of the invention.

FIG. 1 shows a model of BPTI and KD1 (Kunitz domain of TFPI-2) with plasmin. Top shows the sequence alignment of BPTI (SEQ ID NO:5) KD1 (amino acids 10-67 of SEQ ID NO:1) I (SEQ ID NO: 6). Addition of 9 to the sequence will result in KD1 numbering. In the model, plasmin, BPTI and KD1 are shown as ribbons. Plasmin residues are shown with a suffix p. On the left is the BPTI:plasmin complex and on the right is the KD1:plasmin complex. Residues 9,11,22,33 and 35 both in the BPTI and KD1 form the hydrophobic core. The hydrophobic patch in BPTI as well as in KD1 comprised of residues 17, 8, 19, and 34 is shown interacting with the hydrophobic patch in plasmin consisting of residues 37{583}, 39{585}, and 41 {587}. Glu39 of the acidic patch in KD1 interacts directly with Arg175 {719} and possibly through water molecules to Arg100 {644} and Arg221 {767} of the basic patch in plasmin; since in BPTI residue 39 is Arg, such interactions with plasmin are not possible. Tyr46 of KD1 interacts with Lys60A {607} and Arg60D {610} in plasmin; since residue 46 is Lys in BPTI, such interactions are not possible. Arg17 in BPTI interacts with Glu73 {623} in plasmin; since residue 17 is Leu in KD1, such interaction are not possible. Thr11 in BPTI makes H-bond with the side chain N of Gln192 {738}; since residue 11 is Tyr in KD1, such interactions are not possible. Residue 192 is not shown in the figure. Also not shown is the residue 20, which is Arg in both BPTI and KD1 that interacts with the Glu60 {606} in plasmin. The P1 residue 15 in BPTI is Lys that interacts with the side chain O of Ser190 (736} and Asp189 {735} through a water molecule is shown. The P1 residue 15 in KD1 is Arg that also interacts with Ser190 and Asp 189 in plasmin is shown. The numbering system used for plasmin is that of chymotrypsin. Where insertions occur, the chymotrypsin numbering is followed by a capital letter such as 60A and 60D. The numbers in curly brackets represent plasminogen numbering.

FIG. 2 shows control experiments showing Inhibition of Plasmin by BPTI at different times (0.5 & 1 hr) and substrate (S-2251) concentrations (0.5 & 1 mM). BPTI binds plasmin with an apparent dissociation constant Kd of 1±0.5). Also there does not seem to be any substrate-induced displacement of the bound inhibitor.

FIG. 3 shows inhibition of plasmin by WTKD1 at different times (0.5 and 1 hr) and substrate concentrations (0.5 and 1 mM) WTKD1 binds plasmin with an apparent Kd of 22±2 nM. Also there is not any significant substrate induced displacement of inhibitor.

FIG. 4 shows inhibition of plasmin by WTKD1, R15K/L17R and R15K (note that in the figures, R24K=R15K and L26R=L17R, where R24K and L26R are KD1 numbering, and R15K and L26R are BPTI numbering). The incubation time was 1 hr at 37° C. and substrate concentration was 1 mM for the remaining activity measurements. The R15K/L17R mutant inhibits plasmin with an apparent Kd of 3±1 nM. The R24K mutant inhibits plasmin with a Kd of 9-11 nM. The WT KD1 inhibits plasmin with a Kd of 22 nM, which is two-fold different from the Kd of 10±2 nM for the R24K mutant. The L26R (L17R in BPTI numbering) gave KD value of 6±2, which is ˜4-fold better than the WT KD1.

FIG. 5 shows an example wherein surface activator plus phospholipid was mixed with normal human plasma in equal amounts (75 microliter). Ten microliter of buffer containing inhibitor (KD1 wt, KD1 L26R or BPTI) was added and the sample incubated for five minutes at 37° C. Seventy-five microliter of 25 mM CaCl₂ prewarmed to 37° C. was then added and the time needed to form the clot through the intrinsic pathway of blood coagulation was noted. The data show that KD1 WT and BPTI each inhibit the intrinsic pathway of coagulation whereas L26R mutant (L17R in BPTI numbering) of KD1 is ineffective in this regard. Similarly, the extrinsic pathway of coagulation is expected not to be inhibited by the L26R change.

FIG. 6 shows both wt KD1 and L26R inhibited mouse plasmin effectively. The WtKd1 and the L26R mutant are quite effective in inhibiting mouse plasmin with an apparent KD value of ˜80 nM. Complete inhibition was obtained at 1 μM for both wt and L26R KD1.

DETAILED DESCRIPTION OF THE INVENTION

The present invention may be understood more readily by reference to the following detailed description of preferred embodiments of the invention and the examples included therein and to the figures and their previous as well as the following description.

A. DEFINITIONS

As used in the specification and the appended claims, the singular forms “a,” “an” and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to “a small molecule” includes mixtures of one or more small molecules, and the like.

Ranges may be expressed herein as from “about” one particular value, and/or to “about” another particular value. When such a range is expressed, another embodiment includes from the one particular value and/or to the other particular value. Similarly, when values are expressed as approximations, by use of the antecedent “about,” it will be understood that the particular value forms another embodiment. It will be further understood that the endpoints of each of the ranges are significant both in relation to the other endpoint, and independently of the other endpoint.

The terms “higher,” “increases,” “elevates,” or “elevation” refer to increases above basal levels, e.g., as compared to a control. The terms “low,” “lower,” “reduces,” or “reduction” refer to decreases below basal levels, e.g., as compared to a control.

B. METHODS OF USING

Bovine pancreatic trypsin inhibitor (BPTI) is a Kunitz-type serine protease inhibitor. It inhibits plasmin and it is being used in open heart surgery and recommended in orthopaedic surgery to minimize preoperative bleeding and administration of blood products (1-5). Recently, plasminogen/plasmin system has also been implicated in development of the rheumatoid arthritis (6-10) as well as in bone remodeling and resorption (11-15) and tumorogenesis and angiogenesis (8, 16, 17).

Human tissue factor pathway inhibitor-2 (TFPI-2), also known as matrix serine protease inhibitor or placental protein 5, contains three Kunitz-type (similar to BPTI) domains in tandem with a short acidic amino terminus and very basic C-terminal tail (18,19). A variety of cells, including keratinocytes, dermal fibroblasts, smooth muscle cells, syncytiotrophoblasts, synovioblasts, and endothelial cells synthesize and secrete TFPI-2 into the extracellular matrix (ECM) (20-23). TFPI-2 is found in three forms due to differences in glycosylation with Mr 27,000, 30,000 and 32,000(24). First Kunitz domain (KD1) of human TFPI-2 is homologous to BPTI and it also inhibits plasmin (25). Although KD1 is specific for inhibiting plasmin, the other two Kunitz domains in TFPI-2 have no discernable inhibitory activity. The C-terminal basic tail, however, may anchor TFPI-2 to the glycosamine moieties in the ECM for localized inhibition of plasmin.

The crystal structure of BPTI (26) and that of the KD1 (27) with trypsin have been determined. The crystal structure of the protease domain of human plasmin has also been determined (28). Using these structures as templates, the complexes of plasmin with BPTI as well as plasmin and KD1 have been modeled with a high degree of accuracy. The relative positions of the inhibitors and the proteinase domain of plasmin were maintained and minor adjustments were only made in the side chains. Hydrophobic/van der Waals, hydrogen bonds, and ionic interactions were observed between each proteinase-inhibitor complex. All of these interactions were taken into consideration in evaluating each inhibitor-proteinase complex, and it was assumed that all potential hydrogen bond donors and acceptors would participate in these interactions. Bulk solvent was excluded from the proteinase-inhibitor complex and, accordingly, it was anticipated that hydrogen bonds and ionic interactions that may play an important role in specificity could be accurately evaluated. The protocols for modeling these complexes have been described earlier (29).

FIG. 1 depicts the residues in BPTI and KD1 that interacts with plasmin. From the models presented in FIG. 1, changing Leu17 to Arg, and Tyr11 to Thr in KD1 yields a molecule that has significantly higher affinity and specificity towards human plasmin. Changing Tyr46 to Glu and Asp10 to Tyr (or Glu) also increases affinity and specificity towards inhibiting plasmin. On the other hand, changing Glu39 to Arg and Tyr46 to Lys can result in substantial loss of affinity of KD1 for the human plasmin. Systematically, changing those residues that result in gain of function such as modified KD1 with Thr11 and Arg17 yields a molecule that is more potent than BPTI and native KD1. Such a molecule can also be less immunogenic than BPTI. The basic tail to the selective molecule can also be added to the C-terminal containing few extra residues as a linker such that its half-life in the extracellular matrix is increased. Herein disclosed are methods of inhibiting at least one activity of plasmin comprising contacting plasmin with an effective amount of a polypeptide disclosed herein.

Some forms of the disclosed molecules and polypeptides can inhibit plasmin but have reduced anticoagulation activity compared to the wild type Kunitz domain of TFPI-2. Some forms of the disclosed molecules and polypeptides are also specific as antifibrinolytic agents. Thus, some forms of the disclosed molecules and polypeptides are more active as antifibrinoltic agents but no longer have anticoagulant activity or have reduced anticoagulant activity. This property makes such molecules and polypeptides quite useful for preventing bleeding.

Also disclosed is a method of treating a subject in need of inhibition of a plasmin activity, comprising administering to the subject an effective amount of a polypeptide disclosed herein. Examples of diseases, disorders, and treatments relating to the need of inhibition of plasmin include, but are not limited to, tumorogenesis, angiogenesis, bone remodeling, surgery, hemophilia, orthopedic surgery, coronary artery bypass grafting (CABG), and systemic inflammatory response syndrome (SIRS).

Also disclosed is a method of treating rheumatoid arthritis in a subject in need thereof, comprising administering to the subject an effective amount of a polypeptide disclosed herein.

Also disclosed is a method of identifying a plasmin inhibitor comprising: modeling a crystal structure of plamsin with a variant of KD1; determining interaction between the plasmin and the variant of KD1; based on the interaction, determining if the variant of KD1 is a plasmin inhibitor.

Also disclosed is a method of inhibiting plasmin in a subject in need thereof comprising administering to the subject an effective amount of the nucleic acid disclosed herein.

Also disclosed is a method of showing efficacy of a compound for human use in a mosue model of reduced blood loss. It has been discovered that wild-type KD1 and the disclosed mutants both inhibit mouse plasmin (see Example 3). Thus, the mutant can be used to show efficacy in a mouse model of reduced blood loss.

Proteins of this invention may be produced by any conventional technique, including nonbiological synthesis by sequential coupling of components, e.g., amino acids, production by recombinant DNA techniques in suitable host cells, and semisynthesis, for example, by removal of undesired sequences and coupling of synthetic replacement sequences. Proteins disclosed herein are preferably produced, recombinantly, in a suitable host, such as bacteria from the genera Bacillus, Escherichia, Salmonella, Erwinia, and yeasts from the genera Hansenula, Kluyveromyces, Pichia, Rhinosporidium, Saccharomyces, and Schizosaccharomyces, or cultured mammalian cells such as COS-1. The more preferred hosts are microorganisms of the species Pichia pastoris, Bacillus subtilis, Bacillus brevis, Saccharomyces cerevisiae, Escherichia coli and Yarrowia lipolytica. Any promoter which is functional in the host cell may be used to control gene expression.

The proteins can be secreted and can be obtained from conditioned medium. Secretion is the preferred route because proteins are more likely to fold correctly and can be produced in conditioned medium with few contaminants. Secretion is not required.

Proteins designed to lack N-linked glycosylation sites to reduce potential for antigenicity of glycogroups can be used, and so that equivalent proteins can be expressed in a wide variety of organisms including: 1) E. coli, 2) B. subtilis, 3) P. pastoris, 4) S. cerevisiae, and 5) mammalian cells.

Several means exist for reducing the problem of host cells producing proteases that degrade the recombinant product. Overexpression of the B. subtilis signal peptidase in E. coli leads to increased expression of a heterologous fusion protein. It has also been reported that addition of PMSF (a serine proteases inhibitor) to the culture medium improved the yield of a fusion protein.

Other factors that can affect production of these and other proteins disclosed herein include: 1) codon usage (optimizing codons for the host is preferred), 2) signal sequence, 3) amino-acid sequence at intended processing sites, presence and localization of processing enzymes, deletion, mutation, or inhibition of various enzymes that might alter or degrade the engineered product and mutations that make the host more permissive in secretion (permissive secretion hosts are preferred).

Reference works on the general principles of recombinant DNA technology include Watson et al., Molecular Biology of the Gene, Volumes I and II, The Benjamin/Cummings Publishing Company, Inc., Menlo Park, Calif. (1987); Darnell et al., Molecular Cell Biology, Scientific American Books, Inc., New York, N.Y. (1986); Lewin, Genes II, John Wiley & Sons, New York, N.Y. (1985); Old, et al., Principles of Gene Manipulation: An Introduction to Genetic Engineering, 2d edition, University of California Press, Berkeley, Calif. (1981); Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y. (1989); and Ausubel et al, Current Protocols in Molecular Biology, Wiley Interscience, N.Y., (1987, 1992). These references are herein entirely incorporated by reference as are the references cited therein.

Any suitable method can be used to test the compounds of this invention. Scatchard (Ann NY Acad Sci (1949) 51:660-669) described a classical method of measuring and analyzing binding which is applicable to protein binding. This method requires relatively pure protein and the ability to distinguish bound protein from unbound.

A second appropriate method of measuring Kd is to measure the inhibitory activity against the enzyme. If the Kd to be measured is in the 1 nM to 1 μM range, this method requires chromogenic or fluorogenic substrates and tens of micrograms to milligrams of relatively pure inhibitor. For the proteins of this invention, having Kd in the range 5 nM to 50 pM, nanograms to micrograms of inhibitor suffice. When using this method, the competition between the inhibitor and the enzyme substrate can give a measured Ki that is higher than the true Ki.

A third method of determining the affinity of a protein for a second material is to have the protein displayed on a genetic package, such as M13, and measure the ability of the protein to adhere to the immobilized “second material.” This method is highly sensitive because the genetic packages can be amplified. Inhibitors of known affinity for the protease are used to establish standard profiles against which other phage-displayed inhibitors are judged. Any other suitable method of measuring protein binding can also be used.

The proteins of this invention can have a Kd for plasmin of at most about 5 nM, at most about 300 pM, or 100 pM or less. The binding can be inhibitory so that Ki is the same as Kd. The Ki of QS4 for plasmin is about 2 nM. The Ki of SPI11 for plasmin is about 88 pM.

The compositions disclosed herein can be administered in vivo in a pharmaceutically acceptable carrier. By “pharmaceutically acceptable” is meant a material that is not biologically or otherwise undesirable, i.e., the material may be administered to a subject, along with the nucleic acid or vector, without causing any undesirable biological effects or interacting in a deleterious manner with any of the other components of the pharmaceutical composition in which it is contained. The carrier would naturally be selected to minimize any degradation of the active ingredient and to minimize any adverse side effects in the subject, as would be well known to one of skill in the art.

The compositions may be administered orally, parenterally (e.g., intravenously), by intramuscular injection, by intraperitoneal injection, transdermally, extracorporeally, topically or the like, including topical intranasal administration or administration by inhalant. As used herein, “topical intranasal administration” means delivery of the compositions into the nose and nasal passages through one or both of the nares and can comprise delivery by a spraying mechanism or droplet mechanism, or through aerosolization of the nucleic acid or vector. Administration of the compositions by inhalant can be through the nose or mouth via delivery by a spraying or droplet mechanism. Delivery can also be directly to any area of the respiratory system (e.g., lungs) via intubation. The exact amount of the compositions required will vary from subject to subject, depending on the species, age, weight and general condition of the subject, the severity of the allergic disorder being treated, the particular nucleic acid or vector used, its mode of administration and the like. Thus, it is not possible to specify an exact amount for every composition. However, an appropriate amount can be determined by one of ordinary skill in the art using only routine experimentation given the teachings herein.

Parenteral administration of the composition, if used, is generally characterized by injection. Injectables can be prepared in conventional forms, either as liquid solutions or suspensions, solid forms suitable for solution of suspension in liquid prior to injection, or as emulsions. A more recently revised approach for parenteral administration involves use of a slow release or sustained release system such that a constant dosage is maintained. See, e.g., U.S. Pat. No. 3,610,795, which is incorporated by reference herein.

The materials may be in solution, suspension (for example, incorporated into microparticles, liposomes, or cells). These may be targeted to a particular cell type via antibodies, receptors, or receptor ligands. The following references are examples of the use of this technology to target specific proteins to tumor tissue (Senter et al., Bioconjugate Chem., 2:447-451, (1991); Bagshawe, K. D., Br. J. Cancer, 60:275-281, (1989); Bagshawe et al., Br. J. Cancer, 58:700-703, (1988); Senter et al., Bioconjugate Chem., 4:3-9, (1993); Battelli et al., Cancer Immunol. Immunother., 35:421-425, (1992); Pietersz and McKenzie, Immunolog. Reviews, 129:57-80, (1992); and Roffler et al., Biochem. Pharmacol, 42:2062-2065, (1991)). Vehicles such as “stealth” and other antibody conjugated liposomes (including lipid mediated drug targeting to colonic carcinoma), receptor mediated targeting of DNA through cell specific ligands, lymphocyte directed tumor targeting, and highly specific therapeutic retroviral targeting of murine glioma cells in vivo. The following references are examples of the use of this technology to target specific proteins to tumor tissue (Hughes et al., Cancer Research, 49:6214-6220, (1989); and Litzinger and Huang, Biochimica et Biophysica Acta, 1104:179-187, (1992)). In general, receptors are involved in pathways of endocytosis, either constitutive or ligand induced. These receptors cluster in clathrin-coated pits, enter the cell via clathrin-coated vesicles, pass through an acidified endosome in which the receptors are sorted, and then either recycle to the cell surface, become stored intracellularly, or are degraded in lysosomes. The internalization pathways serve a variety of functions, such as nutrient uptake, removal of activated proteins, clearance of macromolecules, opportunistic entry of viruses and toxins, dissociation and degradation of ligand, and receptor-level regulation. Many receptors follow more than one intracellular pathway, depending on the cell type, receptor concentration, type of ligand, ligand valency, and ligand concentration. Molecular and cellular mechanisms of receptor-mediated endocytosis has been reviewed (Brown and Greene, DNA and Cell Biology 10:6, 399-409 (1991)).

The compositions disclosed herein can be used therapeutically in combination with a pharmaceutically acceptable carrier.

Suitable carriers and their formulations are described in Remington: The Science and Practice of Pharmacy (19th ed.) ed. A. R. Gennaro, Mack Publishing Company, Easton, Pa. 1995. Typically, an appropriate amount of a pharmaceutically-acceptable salt is used in the formulation to render the formulation isotonic. Examples of the pharmaceutically-acceptable carrier include, but are not limited to, saline, Ringer's solution and dextrose solution. The pH of the solution is preferably from about 5 to about 8, and more preferably from about 7 to about 7.5. Further carriers include sustained release preparations such as semipermeable matrices of solid hydrophobic polymers containing the antibody, which matrices are in the form of shaped articles, e.g., films, liposomes or microparticles. It will be apparent to those persons skilled in the art that certain carriers may be more preferable depending upon, for instance, the route of administration and concentration of composition being administered.

Pharmaceutical carriers are known to those skilled in the art. These most typically would be standard carriers for administration of drugs to humans, including solutions such as sterile water, saline, and buffered solutions at physiological pH. The compositions can be administered intramuscularly or subcutaneously. Other compounds will be administered according to standard procedures used by those skilled in the art.

Pharmaceutical compositions may include carriers, thickeners, diluents, buffers, preservatives, surface active agents and the like in addition to the molecule of choice. Pharmaceutical compositions may also include one or more active ingredients such as antimicrobial agents, antiinflammatory agents, anesthetics, and the like.

The pharmaceutical composition may be administered in a number of ways depending on whether local or systemic treatment is desired, and on the area to be treated. Administration may be topically (including ophthalmically, vaginally, rectally, intranasally), orally, by inhalation, or parenterally, for example by intravenous drip, subcutaneous, intraperitoneal or intramuscular injection. The disclosed antibodies can be administered intravenously, intraperitoneally, intramuscularly, subcutaneously, intracavity, or transdermally.

Preparations for parenteral administration include sterile aqueous or non-aqueous solutions, suspensions, and emulsions. Examples of non-aqueous solvents are propylene glycol, polyethylene glycol, vegetable oils such as olive oil, and injectable organic esters such as ethyl oleate. Aqueous carriers include water, alcoholic/aqueous solutions, emulsions or suspensions, including saline and buffered media. Parenteral vehicles include sodium chloride solution, Ringer's dextrose, dextrose and sodium chloride, lactated Ringer's, or fixed oils. Intravenous vehicles include fluid and nutrient replenishers, electrolyte replenishers (such as those based on Ringer's dextrose), and the like. Preservatives and other additives may also be present such as, for example, antimicrobials, anti-oxidants, chelating agents, and inert gases and the like.

Formulations for topical administration may include ointments, lotions, creams, gels, drops, suppositories, sprays, liquids and powders. Conventional pharmaceutical carriers, aqueous, powder or oily bases, thickeners and the like may be necessary or desirable.

Compositions for oral administration include powders or granules, suspensions or solutions in water or non-aqueous media, capsules, sachets, or tablets. Thickeners, flavorings, diluents, emulsifiers, dispersing aids or binders may be desirable.

Some of the compositions may potentially be administered as a pharmaceutically acceptable acid- or base-addition salt, formed by reaction with inorganic acids such as hydrochloric acid, hydrobromic acid, perchloric acid, nitric acid, thiocyanic acid, sulfuric acid, and phosphoric acid, and organic acids such as formic acid, acetic acid, propionic acid, glycolic acid, lactic acid, pyruvic acid, oxalic acid, malonic acid, succinic acid, maleic acid, and fumaric acid, or by reaction with an inorganic base such as sodium hydroxide, ammonium hydroxide, potassium hydroxide, and organic bases such as mono-, di-, trialkyl and aryl amines and substituted ethanolamines.

Effective dosages and schedules for administering the compositions may be determined empirically, and making such determinations is within the skill in the art. The dosage ranges for the administration of the compositions are those large enough to produce the desired effect in which the symptoms of the disorder are affected. The dosage should not be so large as to cause adverse side effects, such as unwanted cross-reactions, anaphylactic reactions, and the like. Generally, the dosage will vary with the age, condition, sex and extent of the disease in the patient, route of administration, or whether other drugs are included in the regimen, and can be determined by one of skill in the art. The dosage can be adjusted by the individual physician in the event of any counterindications. Dosage can vary, and can be administered in one or more dose administrations daily, for one or several days. Guidance can be found in the literature for appropriate dosages for given classes of pharmaceutical products.

Proteins of this invention can be applied in vitro to any suitable sample that might contain plasmin to measure the plasmin present. To do so, the assay can include a Signal Producing System (SPS) providing a detectable signal that depends on the amount of plasmin present. The signal may be detected visually or instrumentally. Possible signals include production of colored, fluorescent, or luminescent products, alteration of the characteristics of absorption or emission of radiation by an assay component or product, and precipitation or agglutination of a component or product.

The component of the SPS most intimately associated with the diagnostic reagent is called the “label”. A label may be, e.g., a radioisotope, a fluorophore, an enzyme, a co-enzyme, an enzyme substrate, an electron-dense compound, or an agglutinable particle. A radioactive isotope can be detected by use of, for example, a γ counter or a scintillation counter or by autoradiography. Isotopes which are particularly useful are ³H, ¹²⁵I, ¹³¹I, ³⁵S, ¹⁴C, and, preferably, ¹²⁵I. It is also possible to label a compound with a fluorescent compound. When the fluorescently labeled compound is exposed to light of the proper wave length, its presence can be detected. Among the most commonly used fluorescent labeling compounds are fluorescein isothiocyanate, rhodamine, phycoerythrin, phycocyanin, allophycocyanin, o-phthaldehyde, and fluorescamine. Alternatively, fluorescence-emitting metals, such as 125Eu or other lanthanide, may be attached to the binding protein using such metal chelating groups as diethylenetriaminepentaacetic acid or ethylenediamine-tetraacetic acid. The proteins also can be detectably labeled by coupling to a chemiluminescent compound, such as luminol, isolumino, theromatic acridinium ester, imidazole, acridinium salt, and oxalate ester. Likewise, a bioluminescent compound, such as luciferin, luciferase and aequorin, may be used to label the binding protein. The presence of a bioluminescent protein is determined by detecting the presence of luminescence. Enzyme labels, such as horseradish peroxidase and alkaline phosphatase, are preferred.

There are two basic types of assays: heterogeneous and homogeneous. In heterogeneous assays, binding of the affinity molecule to analyte does not affect the label; thus, to determine the amount of analyte, bound label must be separated from free label. In homogeneous assays, the interaction does affect the activity of the label, and analyte can be measured without separation.

In general, a plasmin-binding protein (PBP) may be used diagnostically in the same way that an antiplasmin antibody is used. Thus, depending on the assay format, it may be used to assay plasmin, or, by competitive inhibition, other substances which bind plasmin.

The sample will normally be a biological fluid, such as blood, urine, lymph, semen, milk, or cerebrospinal fluid, or a derivative thereof, or a biological tissue, e.g., a tissue section or homogenate. The sample could be anything. If the sample is a biological fluid or tissue, it may be taken from a human or other mammal, vertebrate or animal, or from a plant. The preferred sample is blood, or a fraction or derivative thereof.

In one embodiment, the plasmin-binding protein (PBP) is immobilized, and plasmin in the sample is allowed to compete with a known quantity of a labeled or specifically labelable plasmin analogue. The “plasmin analogue” is a molecule capable of competing with plasmin for binding to the PBP, which includes plasmin itself. It may be labeled already, or it may be labeled subsequently by specifically binding the label to a moiety differentiating the plasmin analogue from plasmin. The phases are separated, and the labeled plasmin analogue in one phase is quantified.

In a “sandwich assay,” both an insolubilized plasmin-binding agent (PBA), and a labeled PBA are employed. The plasmin analyte is captured by the insolubilized PBA and is tagged by the labeled PBA, forming a tertiary complex. The reagents may be added to the sample in any order. The PBAs may be the same or different, and only one PBA need be a PBP according to this invention (the other may be, e.g., an antibody). The amount of labeled PBA in the tertiary complex is directly proportional to the amount of plasmin in the sample.

The two embodiments described above are both heterogeneous assays. A homogeneous assay requires only that the label be affected by the binding of the PBP to plasmin. The plasmin analyte may act as its own label if a plasmin inhibitor is used as a diagnostic reagent.

A label may be conjugated, directly or indirectly (e.g., through a labeled anti-PBP antibody), covalently (e.g., with SPDP) or noncovalently, to the plasmin-binding protein, to produce a diagnostic reagent. Similarly, the plasmin binding protein may be conjugated to a solid phase support to form a solid phase (“capture”) diagnostic reagent. Suitable supports include glass, polystyrene, polypropylene, polyethylene, dextran, nylon, amylases, and magnetite. The carrier can be soluble to some extent or insoluble for the purposes of this invention. The support material may have any structure so long as the coupled molecule is capable of binding plasmin.

A Kunitz domain that binds very tightly to plasmin can be used for in vivo imaging. Diagnostic imaging of disease foci was considered one of the largest commercial opportunities for monoclonal antibodies, but this opportunity has not been achieved. Despite considerable effort, only two monoclonal antibody-based imaging agents have been approved. The disappointing results obtained with monoclonal antibodies are due in large measure to: i) inadequate affinity and/or specificity; ii) poor penetration to target sites; iii) slow clearance from nontarget sites; iv) immunogenicity; and v) high production cost and poor stability.

These limitations have led to the development of peptide-based imaging agents. While potentially solving the problems of poor penetration and slow clearance, peptide-based imaging agents are unlikely to possess adequate affinity, specificity and in vivo stability to be useful in most applications.

Engineered proteins are uniquely suited to the requirements for an imaging agent. In particular the extraordinary affinity and specificity that is obtainable by engineering small, stable, human-origin protein domains having known in vivo clearance rates and mechanisms combine to provide earlier, more reliable results, less toxicity/side effects, lower production and storage cost, and greater convenience of label preparation. Indeed, it is possible to achieve the goal of realtime imaging with engineered protein imaging agents. Plasmin-binding proteins, e.g., SPI11, can be useful for localizing sites of internal hemorrhage.

Radio-labeled binding protein may be administered to the human or animal subject. Administration is typically by injection, e.g., intravenous or arterial or other means of administration in a quantity sufficient to permit subsequent dynamic and/or static imaging using suitable radio-detecting devices. The dosage is the smallest amount capable of providing a diagnostically effective image, and may be determined by means conventional in the art, using known radio-imaging agents as guides.

Typically, the imaging is carried out on the whole body of the subject, or on that portion of the body or organ relevant to the condition or disease under study. The radio-labeled binding protein has accumulated. The amount of radio-labeled binding protein accumulated at a given point in time in relevant target organs can then be quantified.

A particularly suitable radio-detecting device is a scintillation camera, such as a γ camera. The detection device in the camera senses and records (and optional digitizes) the radioactive decay. Digitized information can be analyzed in any suitable way, many of which are known in the art. For example, a time-activity analysis can illustrate uptake through clearance of the radio-labeled binding protein by the target organs with time.

Various factors are taken into consideration in picking an appropriate radioisotope. The isotope is picked: to allow good quality resolution upon imaging, to be safe for diagnostic use in humans and animals, and, preferably, to have a short half-life so as to decrease the amount of radiation received by the body. The radioisotope used should preferably be pharmacologically inert, and the quantities administered should not have substantial physiological effect. The binding protein may be radio-labeled with different isotopes of iodine, for example ¹²³I, ¹²⁵I, or ¹³¹I (see, for example, U.S. Pat. No. 4,609,725). The amount of labeling must be suitably monitored.

In applications to human subjects, it may be desirable to use radioisotopes other than ¹²⁵I for labeling to decrease the total dosimetry exposure of the body and to optimize the detectability of the labeled molecule. Considering ready clinical availability for use in humans, preferred radio-labels include: ^(99m)Tc, ⁶⁷Ga, 68Ga, ⁹⁰Y, ¹¹¹In, ^(113m)In, ¹²³I, ¹⁸⁶Re, ¹⁸⁸Re or ²¹¹ At. Radio-labeled protein may be prepared by various methods. These include radio-halogenation by the chloramine-T or lactoperoxidase method and subsequent purification by high pressure liquid chromatography, for example, see Gutkowska et al in “Endocrinology and Metabolism Clinics of America: (1987) 16 (1): 183. Other methods of radio-labeling can be used, such as IODOBEADS^(™.)

A radio-labeled protein may be administered by any means that enables the active agent to reach the agent's site of action in a mammal. Because proteins are subject to digestion when administered orally, parenteral administration, i.e., intravenous subcutaneous, intramuscular, would ordinarily be used to optimize absorption.

The plasmin-binding proteins of this invention may also be used to purify plasmin from a fluid, e.g., blood. For this purpose, the PBP is preferably immobilized on an insoluble support. Such supports include those already mentioned as useful in preparing solid phase diagnostic reagents.

Proteins can be used as molecular weight markers for reference in the separation or purification of proteins. Proteins may need to be denatured to serve as molecular weight markers. A second general utility for proteins is the use of hydrolyzed protein as a nutrient source. Proteins may also be used to increase the viscosity of a solution.

The protein of this invention may be used for any of the foregoing purposes, as well as for therapeutic and diagnostic purposes as discussed further earlier in this specification.

Chemical polypeptide synthesis is known in the art, and methods of solid phase polypeptide synthesis are well-described in the following references, hereby entirely incorporated by reference: (Merrifield, J Amer Chem Soc 85:2149-2154 (1963); Merrifield, Science 232:341-347 (1986); Wade et al., Biopolymers 25:S21-S37 (1986); Fields, Int J Polypeptide Prot Res 35:161 (1990); MilliGen Report Nos. 2 and 2a, Millipore Corporation, Bedford, Mass., 1987) Ausubel et al, supra, and Sambrook et al, supra. Tan and Kaiser (Biochemistry, 1977, 16:1531-41) synthesized BPTI and a homologue eighteen years ago.

As is known in the art, such methods involve blocking or protecting reactive functional groups, such as free amino, carboxyl and thio groups. After polypeptide bond formation, the protective groups are removed. Thus, the addition of each amino acid residue requires several reaction steps for protecting and deprotecting. Current methods utilize solid phase synthesis, wherein the C-terminal amino acid is covalently linked to insoluble resin particles that can be filtered. Reactants are removed by washing the resin particles with appropriate solvents using an automated machine. Various methods, including the “tBoc” method and the “Fmoc” method are well known in the art. See, inter alia, Atherton et al., J Chem Soc Perkin Trans 1:538-546 (1981) and Sheppard et al, Int J Polypeptide Prot Res 20:451-454 (1982).

C. COMPOSITIONS

Disclosed are the components to be used to prepare the disclosed compositions as well as the compositions themselves to be used within the methods disclosed herein. These and other materials are disclosed herein, and it is understood that when combinations, subsets, interactions, groups, etc. of these materials are disclosed that, while specific reference of each various individual and collective combinations and permutation of these compounds may not be explicitly disclosed, each is specifically contemplated and described herein. For example, if a particular amino acid sequence is disclosed and discussed and a number of modifications that can be made to a number of places within the sequence can be made are discussed, specifically contemplated is each and every combination and permutation of the amino acid and the modifications that are possible unless specifically indicated to the contrary. Thus, if a class of molecules A, B, and C are disclosed as well as a class of molecules D, E, and F and an example of a combination molecule, A-D is disclosed, then even if each is not individually recited each is individually and collectively contemplated meaning combinations, A-E, A-F, B-D, B-E, B-F, C-D, C-E, and C-F are considered disclosed. Likewise, any subset or combination of these is also disclosed. Thus, for example, the sub-group of A-E, B-F, and C-E would be considered disclosed. This concept applies to all aspects of this application including, but not limited to, steps in methods of making and using the disclosed compositions. Thus, if there are a variety of additional steps that can be performed it is understood that each of these additional steps can be performed with any specific embodiment or combination of embodiments of the disclosed methods.

Disclosed herein is a polypeptide comprising SEQ ID NO:1 (Kuntz Type Domain 1, or KD1). SEQ ID NO: 1 is represented by the following: DAAQEPTGNNAEICLLPLD GPCRALLLRYYYDRYTQSCRQFLYGGCEGNANNFYTWEACDDACWRIEKVPKV.

Also disclosed are polypeptides comprising SEQ ID NO:2 (wherein the leucine at position 17 as numbered in BPTI has been changed to arginine): DAAQEPTGNNAEICLL PLDYGPCRARLLRYYYDRYTQSCRQFLYGGCEGNANNFYTWEACDDACWRIEKVPK V.

Also disclosed is SEQ ID NO:3, which is a shorter polypeptide than SEQ ID NO: 1, and also comprises the change at position 17 (L17R): NAEICLLPLDYGPCRAR LLRYYYDRYTQSCRQFLYGGCEGNANNFYTWEACDDACWRIE.

Also disclosed are polypeptides comprising SEQ ID NO:4 (wherein the leucine at position 17 as numbered in BPTI has been changed to arginine and the alanine at position 16 has been changed to methionine): DAAQEPTGNNAEICLLPLDYGPC RMRLLRYYYDRYTQSCRQFLYGGCEGNANNFYTWEACDDACWRIEKVPKV.

It has been discovered that a change from the hydrophobic amino acid at position 17 (leucine) to a charged amino acid such as arginine or lysine affects the anticoagulation activity of KD1 without significantly reducing plasmin inhibition. Particularly useful are such mutant polypeptides where anticoagulation activity is eliminated and plasmin inhibition is increased. Thus, inclusion of a charged or polar amino acid at position 17 is specifically contemplated herein.

The polypeptide of SEQ ID NO:1 can also comprise one or more additional mutations. As disclosed herein, a mutation can be an addition, deletion, or substitution of an amino acid. For example, in addition to the change of leucine to arginine at position 17, the amino acid sequence can also comprise the change of arginine to lysine at position 15, the change of alanine to methionine at position 16, or both. Examples of other changes at position 15 can be found, for example, in U.S. Pat. No. 4,595,674, herein incorporated by reference in its entirety.

Also disclosed herein is a polypeptide comprising SEQ ID NO:1, wherein tyrosine is changed to glutamic acid at position 46. In another embodiment, tyrosine can be changed to threonine at position 11. In another embodiment, aspartic acid can be changed to tyrosine or glutamic acid at position 10. These polypeptides can also comprise one or more additional mutations, such as those discussed above. To summarize, examples of amino acid changes to SEQ ID NO:1 can be found in Table 1. These are only examples, and one of skill in the art would understand that any of these mutations could be used alone or in combination with the other mutations listed herein, or with others not listed, in any permutation or combination possible.

TABLE 1 Mutations of SEQ ID NO: 1 R15K L17R L17K D10Y D10E Y11T Y46E A16G A16M A16S

Also disclosed are compositions and nucleic acids corresponding to the polypeptides discussed herein. A discussion of nucleic acids, compositions, and methods of administration is below. Also disclosed are nucleic acids encoding the polypeptides disclosed herein.

Disclosed herein are polypeptides and their corresponding nucleic acids. It is understood that one way to define any known variants and derivatives or those that might arise of the disclosed nucleic acids and proteins herein is through defining the variants and derivatives in terms of homology to specific known sequences. For example SEQ ID NO:1 sets forth a particular sequence of KD1, and SEQ ID NO:2 sets forth a particular sequence of KD1 containing a mutation. One of ordinary skill in the art at the time of the invention would have understood that other mutations can occur in both the nucleic acid and the protein of the wild type. Some mutations thereof that would not affect its functionality, while others can affect the functionality in a positive way, and are therefore selected for. Specifically disclosed are variants of these and other genes and proteins herein disclosed which have at least, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99 percent homology to the stated sequence. Those of skill in the art readily understand how to determine the homology of two proteins or nucleic acids, such as genes. For example, the homology can be calculated after aligning the two sequences so that the homology is at its highest level.

Another way of calculating homology can be performed by published algorithms. Optimal alignment of sequences for comparison may be conducted by the local homology algorithm of Smith and Waterman Adv. Appl. Math. 2: 482 (1981), by the homology alignment algorithm of Needleman and Wunsch, J. MoL Biol. 48: 443 (1970), by the search for similarity method of Pearson and Lipman, Proc. Natl. Acad. Sci. U.S.A. 85: 2444 (1988), by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, Wis.), or by inspection.

The same types of homology can be obtained for nucleic acids by for example the algorithms disclosed in Zuker, M. Science 244:48-52, 1989, Jaeger et al. Proc. Natl. Acad. Sci. USA 86:7706-7710, 1989, Jaeger et al. Methods Enzymol. 183:281-306, 1989 which are herein incorporated by reference for at least material related to nucleic acid alignment.

There are molecules disclosed herein that are nucleic acid based, including for example the nucleic acids that encode, for example, KD1 as well as any other proteins disclosed herein, as well as various functional nucleic acids. The disclosed nucleic acids are made up of for example, nucleotides, nucleotide analogs, or nucleotide substitutes. Non-limiting examples of these and other molecules are discussed herein. It is understood that for example, when a vector is expressed in a cell, that the expressed mRNA will typically be made up of A, C, G, and U.

A nucleotide is a molecule that contains a base moiety, a sugar moiety and a phosphate moiety. Nucleotides can be linked together through their phosphate moieties and sugar moieties creating an internucleoside linkage. The base moiety of a nucleotide can be adenin-9-yl (A), cytosin-1-yl (C), guanin-9-yl (G), uracil-1-yl (U), and thymin-1-yl (T). The sugar moiety of a nucleotide is a ribose or a deoxyribose. The phosphate moiety of a nucleotide is pentavalent phosphate. An non-limiting example of a nucleotide would be 3′-AMP (3′-adenosine monophosphate) or 5′-GMP (5′-guanosine monophosphate).

A nucleotide analog is a nucleotide which contains some type of modification to either the base, sugar, or phosphate moieties. Modifications to nucleotides are well known in the art and would include for example, 5-methylcytosine (5-me-C), 5-hydroxymethyl cytosine, xanthine, hypoxanthine, and 2-aminoadenine as well as modifications at the sugar or phosphate moieties.

Nucleotide substitutes are molecules having similar functional properties to nucleotides, but which do not contain a phosphate moiety, such as peptide nucleic acid (PNA). Nucleotide substitutes are molecules that will recognize nucleic acids in a Watson-Crick or Hoogsteen manner, but which are linked together through a moiety other than a phosphate moiety. Nucleotide substitutes are able to conform to a double helix type structure when interacting with the appropriate target nucleic acid. It is also possible to link other types of molecules (conjugates) to nucleotides or nucleotide analogs to enhance for example, cellular uptake. Conjugates can be chemically linked to the nucleotide or nucleotide analogs. Such conjugates include but are not limited to lipid moieties such as a cholesterol moiety. (Letsinger et al., Proc. Natl. Acad. Sci. USA, 1989, 86, 6553-6556).

A Watson-Crick interaction is at least one interaction with the Watson-Crick face of a nucleotide, nucleotide analog, or nucleotide substitute. The Watson-Crick face of a nucleotide, nucleotide analog, or nucleotide substitute includes the C2, N1, and C6 positions of a purine based nucleotide, nucleotide analog, or nucleotide substitute and the C2, N3, C4 positions of a pyrimidine based nucleotide, nucleotide analog, or nucleotide substitute.

A Hoogsteen interaction is the interaction that takes place on the Hoogsteen face of a nucleotide or nucleotide analog, which is exposed in the major groove of duplex DNA. The Hoogsteen face includes the N7 position and reactive groups (NH2 or O) at the C6 position of purine nucleotides.

There are a variety of sequences related to, for example, KD1 and mutations thereof, as well as any other protein disclosed herein that are disclosed on Genbank, and these sequences and others are herein incorporated by reference in their entireties as well as for individual subsequences contained therein.

A variety of sequences are provided herein and these and others can be found in Genbank, at www.pubmed.gov. Those of skill in the art understand how to resolve sequence discrepancies and differences and to adjust the compositions and methods relating to a particular sequence to other related sequences. Primers and/or probes can be designed for any sequence given the information disclosed herein and known in the art.

Disclosed are compositions including primers and probes, which are capable of interacting with the genes disclosed herein. In certain embodiments the primers are used to support DNA amplification reactions. Typically the primers will be capable of being extended in a sequence specific manner. Extension of a primer in a sequence specific manner includes any methods wherein the sequence and/or composition of the nucleic acid molecule to which the primer is hybridized or otherwise associated directs or influences the composition or sequence of the product produced by the extension of the primer. Extension of the primer in a sequence specific manner therefore includes, but is not limited to, PCR, DNA sequencing, DNA extension, DNA polymerization, RNA transcription, or reverse transcription. Techniques and conditions that amplify the primer in a sequence specific manner are preferred. In certain embodiments the primers are used for the DNA amplification reactions, such as PCR or direct sequencing. It is understood that in certain embodiments the primers can also be extended using non-enzymatic techniques, where for example, the nucleotides or oligonucleotides used to extend the primer are modified such that they will chemically react to extend the primer in a sequence specific manner. Typically the disclosed primers hybridize with the nucleic acid or region of the nucleic acid or they hybridize with the complement of the nucleic acid or complement of a region of the nucleic acid.

Disclosed herein are methods of treating a subject comprising administering to the subject in need thereof a nucleic acid. For example, disclosed herein are methods of delivering a nucleic acid encoding a mutant of KD1, such as those disclosed herein. These methods include the administration and uptake of exogenous DNA into the cells of a subject (i.e., gene transduction or transfection). The disclosed nucleic acids can be in the form of naked DNA or RNA, or the nucleic acids can be in a vector for delivering the nucleic acids to the cells, whereby the antibody-encoding DNA fragment is under the transcriptional regulation of a promoter, as would be well understood by one of ordinary skill in the art. The vector can be a commercially available preparation, such as an adenovirus vector (Quantum Biotechnologies, Inc. (Laval, Quebec, Canada). Delivery of the nucleic acid or vector to cells can be via a variety of mechanisms. As one example, delivery can be via a liposome, using commercially available liposome preparations such as LIPOFECTIN®, LIPOFECTAMINE® (GIBCO-BRL, Inc., Gaithersburg, Md.), SUPERFECT® (Qiagen, Inc. Hilden, Germany) and TRANSFECTAM® (Promega Biotec, Inc., Madison, Wis.), as well as other liposomes developed according to procedures standard in the art. In addition, the disclosed nucleic acid or vector can be delivered in vivo by electroporation, the technology for which is available from Genetronics, Inc. (San Diego, Calif.) as well as by means of a SONOPORATION™ machine (ImaRx Pharmaceutical Corp., Tucson, Ariz.).

As one example, vector delivery can be via a viral system, such as a retroviral vector system which can package a recombinant retroviral genome (see e.g., Pastan et al., Proc. Natl. Acad. Sci. U.S.A. 85:4486, 1988; Miller et al., Mol. Cell. Biol. 6:2895, 1986). The recombinant retrovirus can then be used to infect and thereby deliver to the infected cells nucleic acid encoding a broadly neutralizing antibody (or active fragment thereof). The exact method of introducing the altered nucleic acid into mammalian cells is, of course, not limited to the use of retroviral vectors. Other techniques are widely available for this procedure including the use of adenoviral vectors (Mitani et al., Hum. Gene Ther. 5:941-948, 1994), adeno-associated viral (AAV) vectors (Goodman et al., Blood 84:1492-1500, 1994), lentiviral vectors (Naidini et al., Science 272:263-267, 1996), pseudotyped retroviral vectors (Agrawal et al., Exper. Hematol. 24:738-747, 1996). Physical transduction techniques can also be used, such as liposome delivery and receptor-mediated and other endocytosis mechanisms (see, for example, Schwartzenberger et al., Blood 87:472-478, 1996). This disclosed compositions and methods can be used in conjunction with any of these or other commonly used gene transfer methods.

As one example, if the antibody-encoding nucleic acid is delivered to the cells of a subject in an adenovirus vector, the dosage for administration of adenovirus to humans can range from about 107 to 109 plaque forming units (pfu) per injection but can be as high as 1012 pfu per injection (Crystal, Hum. Gene Ther. 8:985-1001, 1997; Alvarez and Curiel, Hum. Gene Ther. 8:597-613, 1997). A subject can receive a single injection, or, if additional injections are necessary, they can be repeated at six month intervals (or other appropriate time intervals, as determined by the skilled practitioner) for an indefinite period and/or until the efficacy of the treatment has been established.

Parenteral administration of the nucleic acid or vector, if used, is generally characterized by injection. Injectables can be prepared in conventional forms, either as liquid solutions or suspensions, solid forms suitable for solution of suspension in liquid prior to injection, or as emulsions. A more recently revised approach for parenteral administration involves use of a slow release or sustained release system such that a constant dosage is maintained. See, e.g., U.S. Pat. No. 3,610,795, which is incorporated by reference herein. For additional discussion of suitable formulations and various routes of administration of therapeutic compounds, see, e.g., Remington: The Science and Practice of Pharmacy (19th ed.) ed. A. R. Gennaro, Mack Publishing Company, Easton, Pa. 1995.

As discussed herein there are numerous variants of the KD1 protein that are known and herein contemplated. Specifically, disclosed are mutations of KD1 that are preferable in view of the wild type, such as SEQ ID NO:2. In addition to the functional KD1 variants disclosed herein, there are derivatives of the KD1 protein which also function with those disclosed herein, and are herein contemplated. Protein variants and derivatives are well understood to those of skill in the art and in can involve amino acid sequence modifications. For example, amino acid sequence modifications typically fall into one or more of three classes: substitutional, insertional or deletional variants. Insertions include amino and/or carboxyl terminal fusions as well as intrasequence insertions of single or multiple amino acid residues. Insertions ordinarily will be smaller insertions than those of amino or carboxyl terminal fusions, for example, on the order of one to four residues. Immunogenic fusion protein derivatives, such as those described in the examples, are made by fusing a polypeptide sufficiently large to confer immunogenicity to the target sequence by cross-linking in vitro or by recombinant cell culture transformed with DNA encoding the fusion. Deletions are characterized by the removal of one or more amino acid residues from the protein sequence. Typically, no more than about from 2 to 6 residues are deleted at any one site within the protein molecule. These variants ordinarily are prepared by site specific mutagenesis of nucleotides in the DNA encoding the protein, thereby producing DNA encoding the variant, and thereafter expressing the DNA in recombinant cell culture. Techniques for making substitution mutations at predetermined sites in DNA having a known sequence are well known, for example M13 primer mutagenesis and PCR mutagenesis. Amino acid substitutions are typically of single residues, but can occur at a number of different locations at once; insertions usually will be on the order of about from 1 to 10 amino acid residues; and deletions will range about from 1 to 30 residues. Deletions or insertions preferably are made in adjacent pairs, i.e. a deletion of 2 residues or insertion of 2 residues. Substitutions, deletions, insertions or any combination thereof may be combined to arrive at a final construct. The mutations must not place the sequence out of reading frame and preferably will not create complementary regions that could produce secondary mRNA structure. Substitutional variants are those in which at least one residue has been removed and a different residue inserted in its place. Such substitutions generally are made in accordance with the following Table and are referred to as conservative substitutions.

TABLE 2 Amino Acid Substitutions Original Residue Exemplary Conservative Substitutions, others are known in the art. Ala; ser Arg; lys, gln Asn; gln; his Asp; glu Cys; ser Gln; asn, lys Glu; asp Gly; pro His; asn; gln Ile; leu; val Leu; ile; val Lys; arg; gln Met; leu; ile Phe; met; leu; tyr Ser; thr Thr; ser Trp; tyr Tyr; trp; phe Val; ile; leu

Substantial changes in function or immunological identity are made by selecting substitutions that are less conservative than those in Table 2, i.e., selecting residues that differ more significantly in their effect on maintaining (a) the structure of the polypeptide backbone in the area of the substitution, for example as a sheet or helical conformation, (b) the charge or hydrophobicity of the molecule at the target site or (c) the bulk of the side chain. The substitutions which in general are expected to produce the greatest changes in the protein properties will be those in which (a) a hydrophilic residue, e.g. seryl or threonyl, is substituted for (or by) a hydrophobic residue, e.g. leucyl, isoleucyl, phenylalanyl, valyl or alanyl; (b) a cysteine or proline is substituted for (or by) any other residue; (c) a residue having an electropositive side chain, e.g., lysyl, arginyl, or histidyl, is substituted for (or by) an electronegative residue, e.g., glutamyl or aspartyl; or (d) a residue having a bulky side chain, e.g., phenylalanine, is substituted for (or by) one not having a side chain, e.g., glycine, in this case, (e) by increasing the number of sites for sulfation and/or glycosylation.

For example, the replacement of one amino acid residue with another that is biologically and/or chemically similar is known to those skilled in the art as a conservative substitution. For example, a conservative substitution would be replacing one hydrophobic residue for another, or one polar residue for another. The substitutions include combinations such as, for example, Gly, Ala; Val, Ile, Leu; Asp, Glu; Asn, Gln; Ser, Thr; Lys, Arg; and Phe, Tyr. Such conservatively substituted variations of each explicitly disclosed sequence are included within the mosaic polypeptides provided herein.

Substitutional or deletional mutagenesis can be employed to insert sites for N-glycosylation (Asn-X-Thr/Ser) or O-glycosylation (Ser or Thr). Deletions of cysteine or other labile residues also may be desirable. Deletions or substitutions of potential proteolysis sites, e.g. Arg, is accomplished for example by deleting one of the basic residues or substituting one by glutaminyl or histidyl residues.

Certain post-translational derivatizations are the result of the action of recombinant host cells on the expressed polypeptide. Glutaminyl and asparaginyl residues are frequently post-translationally deamidated to the corresponding glutamyl and asparyl residues. Alternatively, these residues are deamidated under mildly acidic conditions. Other post-translational modifications include hydroxylation of proline and lysine, phosphorylation of hydroxyl groups of seryl or threonyl residues, methylation of the o-amino groups of lysine, arginine, and histidine side chains (T. E. Creighton, Proteins: Structure and Molecular Properties, W. H. Freeman & Co., San Francisco pp 79-86 [1983]), acetylation of the N-terminal amine and, in some instances, amidation of the C-terminal carboxyl.

It is understood that one way to define the variants and derivatives of the disclosed proteins herein is through defining the variants and derivatives in terms of homology/identity to specific known sequences. For example, SEQ ID NO:1 sets forth a particular sequence of KD1, and SEQ ID NO:2 sets forth a particular sequence of a mutant thereof Specifically disclosed are variants of these and other proteins herein disclosed which have at least 70% or 75% or 80% or 85% or 90% or 95% homology to the stated sequence. Those of skill in the art readily understand how to determine the homology of two proteins. For example, the homology can be calculated after aligning the two sequences so that the homology is at its highest level. Another way of calculating homology can be performed by published algorithms. Optimal alignment of sequences for comparison may be conducted by the local homology algorithm of Smith and Waterman Adv. Appl. Math. 2: 482 (1981), by the homology alignment algorithm of Needleman and Wunsch, J. MoL Biol. 48: 443 (1970), by the search for similarity method of Pearson and Lipman, Proc. Natl. Acad. Sci. U.S.A. 85: 2444 (1988), by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, Wis.), or by inspection.

The same types of homology can be obtained for nucleic acids by for example the algorithms disclosed in Zuker, M. Science 244:48-52, 1989, Jaeger et al. Proc. Natl. Acad. Sci. USA 86:7706-7710, 1989, Jaeger et al. Methods Enzymol. 183:281-306, 1989 which are herein incorporated by reference for at least material related to nucleic acid alignment.

It is understood that the description of conservative mutations and homology can be combined together in any combination, such as embodiments that have at least 70% homology to a particular sequence wherein the variants are conservative mutations.

As this specification discusses various proteins and protein sequences it is understood that the nucleic acids that can encode those protein sequences are also disclosed. This would include all degenerate sequences related to a specific protein sequence, i.e. all nucleic acids having a sequence that encodes one particular protein sequence as well as all nucleic acids, including degenerate nucleic acids, encoding the disclosed variants and derivatives of the protein sequences. Thus, while each particular nucleic acid sequence may not be written out herein, it is understood that each and every sequence is in fact disclosed and described herein through the disclosed protein sequence. It is also understood that while no amino acid sequence indicates what particular DNA sequence encodes that protein within an organism, where particular variants of a disclosed protein are disclosed herein, the known nucleic acid sequence that encodes that protein in the particular region from which that protein arises is also known and herein disclosed and described.

It is understood that there are numerous amino acid and peptide analogs which can be incorporated into the disclosed compositions. For example, there are numerous D amino acids or amino acids which have a different functional substituent than those shown in Table 2. The opposite stereo isomers of naturally occurring peptides are disclosed, as well as the stereo isomers of peptide analogs. These amino acids can readily be incorporated into polypeptide chains by charging tRNA molecules with the amino acid of choice and engineering genetic constructs that utilize, for example, amber codons, to insert the analog amino acid into a peptide chain in a site specific way. See, for example, (Thorson et al., Methods in Molec. Biol. 77:43-73 (1991), Zoller, Current Opinion in Biotechnology, 3:348-354 (1992); Ibba, Biotechnology & Genetic Engineering Reviews 13:197-216 (1995), Cahill et al., TIBS, 14 (10):400-403 (1989); Benner, TIB Tech, 12:158-163 (1994); Ibba and Hennecke, Bio/technology, 12:678-682 (1994) all of which are herein incorporated by reference at least for material related to amino acid analogs).

Molecules can be produced that resemble peptides, but which are not connected via a natural peptide linkage. For example, linkages for amino acids or amino acid analogs can include CH2NH—, —CH2S—, —CH2—CH2—, —CH═CH— (cis and trans), —COCH2—, —CH(OH)CH2—, and —CHH2SO— (These and others can be found in Spatola, A. F. in Chemistry and Biochemistry of Amino Acids, Peptides, and Proteins, B. Weinstein, eds., Marcel Dekker, New York, p. 267 (1983); Spatola, A. F., Vega Data (March 1983), Vol. 1, Issue 3, Peptide Backbone Modifications (general review); Morley, Trends Pharm Sci (1980) pp. 463-468; Hudson, D. et al., Int J Pept Prot Res 14:177-185 (1979) (—CH2NH—, CH2CH2—); Spatola et al. Life Sci 38:1243-1249 (1986) (—CH H2—S); Hann J. Chem. Soc Perkin Trans. I 307-314 (1982) (—CH—CH—, cis and trans); Almquist et al. J. Med. Chem. 23:1392-1398 (1980) (—COCH2—); Jennings-White et al. Tetrahedron Lett 23:2533 (1982) (—COCH2—); Szelke et al. European Appln, EP 45665 CA (1982): 97:39405 (1982) (—CH(OH)CH2—); Holladay et al. Tetrahedron. Lett 24:4401-4404 (1983) (—C(OH)CH2—); and Hruby Life Sci 31:189-199 (1982) (—CH2—S—); each of which is incorporated herein by reference. A particularly preferred non-peptide linkage is —CH2NH—. It is understood that peptide analogs can have more than one atom between the bond atoms, such as b-alanine, g-aminobutyric acid, and the like.

Amino acid analogs and analogs and peptide analogs often have enhanced or desirable properties, such as, more economical production, greater chemical stability, enhanced pharmacological properties (half-life, absorption, potency, efficacy, etc.), altered specificity (e.g., a broad-spectrum of biological activities), reduced antigenicity, and others.

D-amino acids can be used to generate more stable peptides, because D amino acids are not recognized by peptidases and such. Systematic substitution of one or more amino acids of a consensus sequence with a D-amino acid of the same type (e.g., D-lysine in place of L-lysine) can be used to generate more stable peptides. Cysteine residues can be used to cyclize or attach two or more peptides together. This can be beneficial to constrain peptides into particular conformations. (Rizo and Gierasch Ann. Rev. Biochem. 61:387 (1992), incorporated herein by reference).

Disclosed are methods of making a transgenic organism comprising administering the disclosed nucleic acids, vectors and/or cells.

The present invention is more particularly described in the following examples, which are intended as illustrative only since numerous modifications and variations therein will be apparent to those skilled in the art.

Although the present process has been described with reference to specific details of certain embodiments thereof, it is not intended that such details should be regarded as limitations upon the scope of the invention except as and to the extent that they are included in the accompanying claims.

The following examples are put forth so as to provide those of ordinary skill in the art with a complete disclosure and description of how the compounds, compositions, articles, devices and/or methods claimed herein are made and evaluated, and are intended to be purely exemplary of the invention and are not intended to limit the scope of what the inventors regard as their invention. Efforts have been made to ensure accuracy with respect to numbers (e.g., amounts, temperature, etc.), but some errors and deviations should be accounted for. Unless indicated otherwise, parts are parts by weight, temperature is in ° C. or is at ambient temperature, and pressure is at or near atmospheric.

D. EXAMPLES 1. Example 1

Materials and methods: The chromogenic substrates H-D-Val-Leu-Lys-p-nitroanilide (S-2251) was purchased from DiaPharma Group Inc. (West Chester, Ohio). Human plasmin was purchased from Enzyme research laborotories. Bovine aprotinin (BPTI) was used from Zymogenetics. Escherichia coli strain BL21 (DE3) pLys and pET28a expression vector were products of Novagen Inc. (Madison, Wis.). The QuikChange® site-directed mutagenesis kit was obtained from Stratagene (La Jolla, Calif.).

Expression and Purification of Wild type and Mutant Proteins. The first Kunitz-type proteinase inhibitor domain of human TFPI-2 (KD1) was cloned into pET28a vector containing a His tag. The mutants were obtained by site directed mutagenesis. The proteins were overexpressed as N-terminal His-tagged fusion proteins in E. coli strain BL21 (DE3) pLys S. using the T7 promoter system. The overexpressed proteins were recovered as inclusion bodies and proteins were folded and purified free of his Tag (27). The concentrations were determined by UV spectroscopy.

Plasmin Inhibition Assays. Plasmin inhibition assays were performed by incubating plasmin with various concentrations of inhibitor preparations (BPTI, KD1WT, KD1 mutants R24K, L26R or R24K/L26R) in 50 mM Tris-HCl, pH 7.5 containing 100 mM NaCl, 0.1 mg/mL BSA, 5 mM CaCl₂ for 1 hr at 37° C. in a 96-well microtitre plate. The chromogenic substrate S-2251 was then added, and residual amidolytic activity was measured in a Molecular Devices UVmax kinetic microplate reader at different end points (0.5 and 1 hr) and S2251 (0.5 and 1 mM) concentrations. Plasmin inhibitory data were analyzed according to the quadratic binding expression.

In control experiments, it was first studied if there was any substrate-induced displacement of bound inhibitor by increasing substrate concentrations. Both BPTI (FIG. 2) and WTKD1 (FIG. 3) were assayed and our results show that there is apparently no displacement of bound inhibitor by increasing substrate concentrations. It was also tested whether or not increased time of incubation of inhibitor with plasmin would result in enhanced inhibition. This was not the case either (FIG. 2 and FIG. 3). These results validate the results presented in FIG. 4. The results obtained from the plasmin inhibitory studies show that the mutant R15K/L17R is a potent inhibitor of plasmin and inhibits plasmin manifold strongly than either the wild type KD1 or the R24K mutant (FIG. 4). Ki* (inhibitory constant) values of 22 nM for WT, 10 nM for R15K, 6 nM for L26R and 3 nM for the R15K/L17R were obtained. Thus L17R change is very important. The L17R change was made based upon molecular modeling. The R15K/L17R mutant binds much strongly to plasmin than WTKDI (7-fold) or the R15K (˜2-fold) mutant. The L17R mutants binds plasmin approximately 4-fold stronger than the WT KD1 Thus, L26R or R15K/L17R can replace BPTI in clinical therapeutics.

Throughout this application, various publications are referenced. The disclosures of these publications in their entireties are hereby incorporated by reference into this application in order to more fully describe the state of the art to which this invention pertains.

2. Example 2 Abolishing the Intrinsic Coagulation Inhibitor Activity of Kunitz Domain 1 (KD1) of TFPI-2

Nomenclature Information

R24 (also known as R15) is P1

A25 (also known as A16) is P1′

L26 (also known as L17) is P2′

TFPI-2 inhibits intrinsic coagulation presumably through the inhibition of factor XIa (Petersen et al. Biochemistry. 1996 Jan. 9; 35 (1):266-272). Like all serine proteases, factor XIa cleaves between P1-P1′ residues TRAE or TRVV (P2-P1-P1′-P2′). Thus KD1 WT having Leu (hydrophobic residue like Val) at P2′ position should inhibit factor XIa. Thus changing Leu to Arg at P2′ position should reduce/abrogate this inhibition.

A common procedure to test inhibition of clotting is to examine the aPTT (activated partial thromboplastin time) of normal plasma. In this test, surface activator plus phospholipid was mixed with normal plasma in equal amounts (75 microliter). Ten microliter of buffer containing inhibitor (KD1 wt, KD1 L26R or BPTI) was added and the sample incubated for five minutes at 37° C. Seventy-five microliter of 25 mM CaCl₂ prewarmed to 37° C. was then added and the time needed to form the clot was noted. The data are shown in FIG. 5. In the aPTT system, coagulation is initiated by the activation of factor XII to Factor XIIa by contact phase involving the kallikrein system. Factor XIIa then activates factor XI to factor XIa in the coagulation cascade.

BPTI inhibits kallikrein whereas KD1 WT inhibits both kallikrein and factor XIa (Petersen et al 1996). This can result in the prolongation of the aPTT by BPTI and KD1 WT whereas L26R Mutant of KD1 is expected to inhibit neither as indicated by no inhibition (prolongation) of aPTT (FIG. 5). This observation makes the L26R KD1 a specific inhibitor of plasmin. It also increases its inhibitory potency towards plasmin as well. Thus, L26R KD1 has no effect on clotting and is a more potent inhibitor than the Wt KD1.

The mutant protein L26R loses activity as an anticoagulant and becomes specific as an antifibrinolytic agent. So the mutant is more active as an antifibrinoltic agent but it also is no longer an anticoagulant. This property makes it useful in preventing bleeding.

3. Example 3 Mouse Plasmin Inhibition Data

Both WT KD1 and L26R inhibited mouse plasmin effectively. This is shown in FIG. 6. Clearly the WT KD1 and the L26R mutant are quite effective in inhibiting mouse plasmin with an apparent Kd value of ˜80 nM. Complete inhibition was obtained at 1 μM for both WT and L26R KD1(Masci et al. Blood Coagulation and Fibrinolysis 2000, Vol 11, No 4, pages 385-393, reference herein incorporated in its entirety and for its teachings regarding in vivo plasmin inhibition). Since both the wild-type and the mutant inhibit mouse plasmin, one can use the mutant to show efficacy in vivo in an animal model of bleeding.

A mouse tail vein bleeding model has been described to study the efficacy of a snake plasmin inhibitor (Masci et al; Blood Coagulation and Fibrinolysis 2000, Vol 11, pages 385-393). Using this mouse tail vein bleeding model, compared to saline control, a 67-70% reduction in blood loss was observed when either Aprotinin, WT KD1 or the mutant L26R was administered intravenously at about 100 microgram/mouse. The doses of the plasmin inhibitors used in these experiments were similar to that used during human CPB (cardiopulmonary bypass) surgery, adjusted to the mouse weight. The Animal Ethics Committee of UCLA approved all mice experiments and the dose used in human surgery adjusted to mouse weight was a realistic basis for these initial studies. The serum BUN/Creatinine levels were normal after two days and seven days following administration of the drug. The microscopic examination of tissues revealed no injury to major organs such as kidney, heart and brain. KD1 WT and KD1 L26R reduced blood loss nearly as effectively as Aprotinin. However, this is expected since the dose used may be high enough to not see differences between the different inhibitors (aprotinin, WT KD1 or the L26R mutant). Further the human KD1 L26R could have a better efficacy in humans because it inhibits human plasmin more selectively and does not inhibit coagulation.

REFERENCES

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What is claimed is:
 1. A polypeptide comprising the amino acid sequence set forth in SEQ ID NO:1 or a sequence having at least 79% identity with SEQ ID NO:1, with a leucine to arginine, serine, threonine, asparagine, histidine or lysine substitution at position 17, using BPTI numbering system; wherein the polypeptide inhibits plasmin activity and has decreased anticoagulation activity as compared to a wild type KDI polypeptide.
 2. The polypeptide of claim 1, wherein the amino acid sequence has at least 80% identity to SEQ ID NO:1.
 3. The polypeptide of claim 1, wherein the amino acid sequence has at least 81% identity to SEQ ID NO:1.
 4. The polypeptide of claim 1, wherein the amino acid sequence has at least 82% identity to SEQ ID NO:1.
 5. The polypeptide of claim 2, which comprises a tyrosine to glutamic acid substitution at position
 46. 6. The polypeptide of claim 1, which comprises a tyrosine to threonine substitution at position
 11. 7. The polypeptide of claim 1, which comprises an aspartic acid to tyrosine substitution at position
 10. 8. The polypeptide of claim 1, which comprises an aspartic acid to glutamic acid substitution at position
 10. 9. The polypeptide of claim 1, which comprises an alanine to methionine, glycine or serine substitution at position
 16. 10. The polypeptide of claim 1, which comprises a leucine to arginine substitution at position
 17. 11. The polypeptide of claim 10, which comprises a tyrosine to threonine substitution at position
 11. 12. The polypeptide of claim 1, which comprises one or more mutations selected from the group consisting of: a tyrosine to threonine substitution at position 11, an alanine to methionine, glycine, or serine substitution at position 16, and an aspartic acid to tyrosine or glutamic acid substitution at position
 10. 13. A composition comprising the polypeptide of claim
 1. 14. A nucleic acid encoding the polypeptide of claim
 1. 